A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18096491



Internal ID20663531
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:15667659..15668179hg38UCSC Ensembl
chr3:15709166..15709686hg19UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg38521
hg19521
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6373203
Supporting Variants
Samples
Known GenesANKRD28
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18096491
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00042


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